07/08/2018 CFDA released “management of imported medical devices agent (draft)” and called for public comment

On 2nd August, CFDA released management of imported medical devices agent (draft) for public comment. The draft defined clearly the requirements for agent and also their obligation. The provincial level CFDA should timely gather agent situation, develop agent catalogue and conduct inspection on site and on annual self-examination report.

http://cnda.cfda.gov.cn/WS04/CL2051/329805.html